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	Title	Authors / Editors	Date
unige:114045	Diagnostic utility of 18F-Fluorodeoxyglucose positron emission tomography (FDG-PET) in asymptomatic subjects at increased risk for Alzheimer's disease	Drzezga, Alexander; Altomare, Daniele; Festari, Cristina; Arbizu, Javier; ... Boccardi, Marina	2018
unige:112189	Association Between Oxytocin Receptor Genotype, Maternal Care, and Eating Disorder Behaviours in a Community Sample of Women	Micali, Nadia; Crous-Bou, Marta; Treasure, Janet; Lawson, Elizabeth A	2017
unige:112335	Effects of single genetic variants and polygenic obesity risk scores on disordered eating in adolescents - The HUNT study	Sardahaee, Farzaneh Saeedzadeh; Holmen, Turid Lingaas; Micali, Nadia; Kvaløy, Kirsti	2017
unige:107412	Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology	Ripperger, Tim; Von Bueren, André	2017
unige:108546	Impact of CD14 Polymorphisms on Anti-Apolipoprotein A-1 IgG-Related Coronary Artery Disease Prediction in the General Population	Antiochos, Panagiotis; Marques-Vidal, Pedro; Virzi, Julien; Pagano, Sabrina; ... Vuilleumier, Nicolas	2017
unige:100764	The Elephant in the Room: The Role of Microtubules in Cancer	Cirillo, Luca; Gotta, Monica; Meraldi, Patrick	2017
unige:110680	Cardiovascular risk in patients with rheumatoid arthritis	Lauper, Kim; Gabay, Cem	2017
unige:127792	Genetic loci associated with heart rate variability and their effects on cardiac disease risk	Nolte, Ilja M; Munoz, M Loretto; Tragante, Vinicius; Snieder, Harold; de Geus, Eco J C	2017
unige:110105	Interleukin-33 and RANK-L Interplay in the Alveolar Bone Loss Associated to Periodontitis	Lapérine, Olivier; Cloitre, Alexandra; Caillon, Jocelyne; Huck, Olivier; ... Lesclous, Philippe	2016
unige:88214	An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis	Marchetti, Giovanna; Girelli, Domenico; Zerbinati, Carlotta; Lunghi, Barbara; ... Martinelli, Nicola	2015
unige:89650	Transcript Expression Data from Human Islets Links Regulatory Signals from Genome-Wide Association Studies for Type 2 Diabetes and Glycemic Traits to Their Downstream Effectors	van de Bunt, Martijn; Manning Fox, Jocelyn E; Dai, Xiaoqing; Barrett, Amy; ... Gloyn, Anna L	2015
unige:76382	De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy	Korff, Christian	2015
unige:79657	Prothrombin G20210A mutation and lower extremity peripheral arterial disease: a systematic review and meta-analysis	Vazquez, F; Rodger, M; Carrier, M; Le Gal, G; ... Gandara, E	2015
unige:90582	The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study	Winkler, Thomas W; Justice, Anne E; Graff, Mariaelisa; Barata, Llilda	2015
unige:90270	Whole exome sequencing of a dominant retinitis pigmentosa family identifies a novel deletion in PRPF31	Villanueva, Adda; Willer, Jason R; Bryois, Julien; Dermitzakis, Emmanouil; ... Davis, Erica E	2014
unige:90276	High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms	Kurki, Mitja I; Gaál, Emília Ilona; Kettunen, Johannes; Lappalainen, Tuuli Emilia; ... Jääskeläinen, Juha E	2014
unige:102920	HLA-DRB1 and HLA-DQB1 allele associations in an Albanian patient population with rheumatoid arthritis: correlations with the specific autoantibody markers and inter-population DRB1 allele frequency variability	Prifti-Kurti, Margarita; Nunes, Jose Manuel; Shyti, Erkena; Ylli, Zamira; ... Sulcebe, Genc	2014
unige:40642	Predicting stroke through genetic risk functions: the CHARGE Risk Score Project	Ehret, Georg Benedikt	2014
unige:40645	Genetic implication of a novel thiamine transporter in human hypertension	International Consortium for Blood Pressure Genome-Wide Association Studies	2014
unige:55235	Prédispositions génétiques dans l'allergie médicamenteuse : importance du HLA	Bergmann, Marcel; Villard, Jean; Caubet, Jean-Christoph Roger J-P	2014

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